Canonical Allele Identifier: CA1427018721

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618594A= , CM000665.2:g.186618594A=	GRCh38
NC_000003.11:g.186336383A= , CM000665.1:g.186336383A=	GRCh37
NC_000003.10:g.187819077A=	NCBI36
NG_011436.1:g.10534A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.632A= MANE Select	ENSP00000393887.2:p.Lys211=
ENST00000273784.5:c.635A=	ENSP00000273784.5:p.Lys212=
ENST00000411641.6:c.632A=	ENSP00000393887.2:p.Lys211=
NM_001622.2:c.632A=	NP_001613.2:p.Lys211=
NM_001354571.1:c.635A=	NP_001341500.1:p.Lys212=
NM_001354572.1:c.629A=	NP_001341501.1:p.Lys210=
NM_001354573.1:c.632A=	NP_001341502.1:p.Lys211=
NM_001622.3:c.632A=	NP_001613.2:p.Lys211=
NM_001622.4:c.632A= MANE Select	NP_001613.2:p.Lys211=
NM_001354571.2:c.635A=	NP_001341500.1:p.Lys212=
NM_001354572.2:c.629A=	NP_001341501.1:p.Lys210=
NM_001354573.2:c.632A=	NP_001341502.1:p.Lys211=